Invasive Diagnostic and Therapeutic Management of Cerebral Vasospasm After Aneurysmatic Subarachnoid Hemorrhage
- Conditions
- Cerebral Vasospasm After Subarachnoid Hemorrhage
- Interventions
- Other: Combination of TBA and intraarterial application of vasodilators
- Registration Number
- NCT01400360
- Lead Sponsor
- Johann Wolfgang Goethe University Hospital
- Brief Summary
Cerebral vasospasm(CVS) after subarachnoid hemorrhage (SAH) results in a considerable amount of transient or even permanent neurological deficits and poor outcome of the patients. Transluminal Balloon angioplasty (TBA) or intraarterial application of vasodilators represents a rescue therapy for severe CVS. Indication, duration and efficacy of this treatment, however, is still under debate. Aim of the study is to investigate if such a rescue treatment can significantly reduce new delayed ischemic cerebral deficits after SAH. Hypothesis is that the occurance of delayed infarcts can be reduced by repetetive intraarterial therapy to more than 50 %.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 92
- SAH (WFNS 1-4)
- Perfusion relevant CVS
- Ability for MRI, DSA and intraarterial treatment
- extended cerebral infarcts
- SAH or ICH from AVM or flow associated aneurysm
- Non aneurismal SAH
- Relevant non spastic stenosis of brain supplying arteries
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description invasive Combination of TBA and intraarterial application of vasodilators After proof of perfusion relevant CVS in interventional therapy should be performed as best possible combination from TBA and intraarterial vasodilators additional to the conventional treatment. conventional Combination of TBA and intraarterial application of vasodilators After proof of perfusion relevant CVS only conventional treatment should be performed (no intraarterial therapy).
- Primary Outcome Measures
Name Time Method New infarcts between baseline and final MRI 21 + - 7 days
- Secondary Outcome Measures
Name Time Method Clinical outcome (mRS, Karnofsky) 6 months
Trial Locations
- Locations (4)
Neurochirurgische Klinik der Universität Ulm
🇩🇪Günzburg, Germany
Neurochirurgische Klinik, Universitätsklinik
🇩🇪Düsseldorf, Germany
Klinik für Neurochirurgie, Universitätsklinikum
🇩🇪Mannheim, Germany
Department of Neurosurgery, Johann Wolfgang Goethe-University
🇩🇪Frankfurt am Main, Germany